@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP177718.RAf2VKW_snDeMFYpAQvZvUqSq4Y8kDns1rzzRqZtTgtnM> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .
dgn-np:NP177718.RAf2VKW_snDeMFYpAQvZvUqSq4Y8kDns1rzzRqZtTgtnM130_head {
   this: np:hasAssertion dgn-np:NP177718.RAf2VKW_snDeMFYpAQvZvUqSq4Y8kDns1rzzRqZtTgtnM130_assertion ;
    np:hasProvenance dgn-np:NP177718.RAf2VKW_snDeMFYpAQvZvUqSq4Y8kDns1rzzRqZtTgtnM130_provenance ;
    np:hasPublicationInfo dgn-np:NP177718.RAf2VKW_snDeMFYpAQvZvUqSq4Y8kDns1rzzRqZtTgtnM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP177718.RAf2VKW_snDeMFYpAQvZvUqSq4Y8kDns1rzzRqZtTgtnM130_assertion a np:Assertion .
  dgn-np:NP177718.RAf2VKW_snDeMFYpAQvZvUqSq4Y8kDns1rzzRqZtTgtnM130_provenance a np:Provenance .
  dgn-np:NP177718.RAf2VKW_snDeMFYpAQvZvUqSq4Y8kDns1rzzRqZtTgtnM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP177718.RAf2VKW_snDeMFYpAQvZvUqSq4Y8kDns1rzzRqZtTgtnM130_assertion {
   miriam-gene:10392 a ncit:C16612 .
  lld:C0007114 a ncit:C7057 .
  dgn-gda:DGN8d66e127630a32d35bdf46bad9cee337 sio:SIO_000628 miriam-gene:10392 , lld:C0007114 ;
    a sio:SIO_001121 .
}
dgn-np:NP177718.RAf2VKW_snDeMFYpAQvZvUqSq4Y8kDns1rzzRqZtTgtnM130_provenance {
   dgn-np:NP177718.RAf2VKW_snDeMFYpAQvZvUqSq4Y8kDns1rzzRqZtTgtnM130_assertion dcterms:description "[NOD1/CARD4 and NOD2/CARD15 gene polymorphisms may be associated with altered risk of gastric, colorectal, breast, ovarian, prostate, testicular, lung, laryngeal, liver, gallbladder, biliary tract, pancreatic, small bowel, kidney, urinary bladder cancer, skin cancer, nonthyroid endocrine tumors, lymphoma and leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
    sio:SIO_000772 miriam-pubmed:21745515 ;
    prov:wasDerivedFrom dgn-void:befree-20140225 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
  dgn-void:source_evidence_literature a eco:ECO_0000212 ;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP177718.RAf2VKW_snDeMFYpAQvZvUqSq4Y8kDns1rzzRqZtTgtnM130_publicationInfo {
   this: dcterms:created "2014-10-02T12:33:36+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269> , <http://orcid.org/0000-0002-7534-7661> , <http://orcid.org/0000-0002-9383-528X> , <http://orcid.org/0000-0003-0169-8159> , <http://orcid.org/0000-0003-1244-7654> ;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}